Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasis

Current views show that an impaired balance partly explains the fat accumulation leading to obesity. Fetal malnutrition and early exposure to endocrine-disrupting compounds also contribute to obesity and impaired insulin secretion and/or sensitivity. The liver plays a major role in systemic glucose...

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Main Authors: Gabriella Garruti, Jacek Baj, Angelo Cignarelli, Sebastio Perrini, Francesco Giorgino
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-05-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2023.1154561/full
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author Gabriella Garruti
Jacek Baj
Angelo Cignarelli
Sebastio Perrini
Francesco Giorgino
author_facet Gabriella Garruti
Jacek Baj
Angelo Cignarelli
Sebastio Perrini
Francesco Giorgino
author_sort Gabriella Garruti
collection DOAJ
description Current views show that an impaired balance partly explains the fat accumulation leading to obesity. Fetal malnutrition and early exposure to endocrine-disrupting compounds also contribute to obesity and impaired insulin secretion and/or sensitivity. The liver plays a major role in systemic glucose homeostasis through hepatokines secreted by hepatocytes. Hepatokines influence metabolism through autocrine, paracrine, and endocrine signaling and mediate the crosstalk between the liver, non-hepatic target tissues, and the brain. The liver also synthetizes bile acids (BAs) from cholesterol and secretes them into the bile. After food consumption, BAs mediate the digestion and absorption of fat-soluble vitamins and lipids in the duodenum. In recent studies, BAs act not simply as fat emulsifiers but represent endocrine molecules regulating key metabolic pathways. The liver is also the main site of the production of ketone bodies (KBs). In prolonged fasting, the brain utilizes KBs as an alternative to CHO. In the last few years, the ketogenic diet (KD) became a promising dietary intervention. Studies on subjects undergoing KD show that KBs are important mediators of inflammation and oxidative stress. The present review will focus on the role played by hepatokines, BAs, and KBs in obesity, and diabetes prevention and management and analyze the positive effects of BAs, KD, and hepatokine receptor analogs, which might justify their use as new therapeutic approaches for metabolic and aging-related diseases.
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spelling doaj.art-31675770e1d34a47a9898e9c1eda17042023-05-19T13:00:39ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922023-05-011410.3389/fendo.2023.11545611154561Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasisGabriella Garruti0Jacek Baj1Angelo Cignarelli2Sebastio Perrini3Francesco Giorgino4Unit of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, Department of Precision and Regenerative Medicine, University of Bari Aldo Moro, Bari, ItalyDepartment of Anatomy, Medical University of Lublin, Lublin, PolandUnit of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, Department of Precision and Regenerative Medicine, University of Bari Aldo Moro, Bari, ItalyUnit of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, Department of Precision and Regenerative Medicine, University of Bari Aldo Moro, Bari, ItalyUnit of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, Department of Precision and Regenerative Medicine, University of Bari Aldo Moro, Bari, ItalyCurrent views show that an impaired balance partly explains the fat accumulation leading to obesity. Fetal malnutrition and early exposure to endocrine-disrupting compounds also contribute to obesity and impaired insulin secretion and/or sensitivity. The liver plays a major role in systemic glucose homeostasis through hepatokines secreted by hepatocytes. Hepatokines influence metabolism through autocrine, paracrine, and endocrine signaling and mediate the crosstalk between the liver, non-hepatic target tissues, and the brain. The liver also synthetizes bile acids (BAs) from cholesterol and secretes them into the bile. After food consumption, BAs mediate the digestion and absorption of fat-soluble vitamins and lipids in the duodenum. In recent studies, BAs act not simply as fat emulsifiers but represent endocrine molecules regulating key metabolic pathways. The liver is also the main site of the production of ketone bodies (KBs). In prolonged fasting, the brain utilizes KBs as an alternative to CHO. In the last few years, the ketogenic diet (KD) became a promising dietary intervention. Studies on subjects undergoing KD show that KBs are important mediators of inflammation and oxidative stress. The present review will focus on the role played by hepatokines, BAs, and KBs in obesity, and diabetes prevention and management and analyze the positive effects of BAs, KD, and hepatokine receptor analogs, which might justify their use as new therapeutic approaches for metabolic and aging-related diseases.https://www.frontiersin.org/articles/10.3389/fendo.2023.1154561/fullbile acidsfastingGPBAR1hepatokinesketogenic diet
spellingShingle Gabriella Garruti
Jacek Baj
Angelo Cignarelli
Sebastio Perrini
Francesco Giorgino
Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasis
Frontiers in Endocrinology
bile acids
fasting
GPBAR1
hepatokines
ketogenic diet
title Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasis
title_full Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasis
title_fullStr Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasis
title_full_unstemmed Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasis
title_short Hepatokines, bile acids and ketone bodies are novel Hormones regulating energy homeostasis
title_sort hepatokines bile acids and ketone bodies are novel hormones regulating energy homeostasis
topic bile acids
fasting
GPBAR1
hepatokines
ketogenic diet
url https://www.frontiersin.org/articles/10.3389/fendo.2023.1154561/full
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